Memanti­nium chloride 0.1-hydrate

The crystal structure of the title compound, C12H22N+·Cl−·0.1H2O, consists of (3,5-dimethyl-1-adamantyl)ammonium chloride (memanti­nium chloride) and uncoordinated water mol­ecules. The four six-membered rings of the memanti­nium cation assume typical chair conformations. The Cl− counter-anion links with the memanti­nium cation via N—H⋯Cl hydrogen bonding, forming channels where the disordered crystal water molecules are located. The O atom of the water mol­ecule is located on a threefold rotation axis, its two H atoms symmetrically distributed over six sites; the water mol­ecule links with the Cl− anions via O—H⋯Cl hydrogen bonding

Quantum state transfer through a spin chain in a multi-excitation subspace

We investigate the quality of quantum state transfer through a uniformly coupled antiferromagnetic spin chain in a multi-excitation subspace. The fidelity of state transfer using multi-excitation channels is found to compare well with communication protocols based on the ground state of a spin chain with ferromagnetic interactions. Our numerical results support the conjecture that the fidelity of state transfer through a multi-excitation subspace only depends on the number of initial excitations present in the chain and is independent of the excitation ordering. Based on these results, we describe a communication scheme which requires little effort for preparation.Comment: 5 pages, 4 figure

Triamcinolone acetonide acetate

In the crystal structure of the title compound [systematic name: 2-(4b-fluoro-5-hy­droxy-4a,6a,8,8-tetra­methyl-2-oxo-2,4a,4b,5,6,6a,9a,10,10a,10b,11,12-dodeca­hydro-7,9-dioxa­penta­leno[2,1-a]phenanthren-6b-yl)-2-oxoethyl acetate], C26H33FO7, the mol­ecules are connected by inter­molecular O—H⋯O hydrogen bonds into an infinite supra­molecular chain along the b axis. The mol­ecular framework consists of five condensed rings, including three six-membered rings and two five-membered rings. The cyclo­hexa-2,5-dienone ring is nearly planar [maximum deviation = 0.013 (3) Å], while the cyclo­hexane rings adopt chair conformations. The two five-membered rings, viz. cyclo­pentane and 1,3-dioxolane, display envelope conformations

Bupropion hydro­bromide propanol hemisolvate

The title compound {systematic name: N-[1-(3-chloro­phen­yl)-1-oxopropan-2-yl]-tert-butanaminium bromide propanol hemisolvate}, C13H19ClNO+·Br−·0.5C3H8O, crystallizes with two independent bupropion hydro­bromide ion pairs and a solvent 1-propanol mol­ecule in the asymmetric unit. In both mol­ecules, the expected proton transfer from HBr to the amino group of the bupropion mol­ecule is observed, and intra- and inter­molecular N—H⋯Br hydrogen-bond inter­actions are formed. These inter­actions link the mol­ecules into hydrogen-bond dimers. The side chains of the two cations have slightly different orientations. The 1-propanol solvent mol­ecule is linked to a bromide ion by an O—H⋯Br hydrogen bond